DNA damage tolerance and mutagenesis : the regulation of S. cerevisiae Rev1

DNA damage constantly challenges the integrity of genetic material during the lifetime of every cell. Accurate duplication of DNA and its proper transmission to a new cell are critical to avoid mutations or loss of genetic information that ultimately may cause altered cellular functions, cell death, or uncontrolled growth as in the case of tumor cells. Fortunately, cells possess a multitude of mechanisms to ensure the fidelity of DNA replication and protect against permanent changes to DNA. These mechanisms divide into the categories of DNA repair and DNA damage tolerance, although some of the proteins involved overlap between both mechanisms. DNA repair restores damaged DNA back to the original, unmodified state. Alternatively, the cell may require DNA damage tolerance to temporarily deal with DNA damage during replication. The altered DNA remains as a result of tolerance and is later a candidate for repair. This work focuses on the DNA damage tolerance pathway of tranlesion synthesis (TLS). TLS involves specialized DNA polymerases with the capacity to bypass DNA lesions that are otherwise inhibitory to replicative polymerases. Specifically, the TLS polymerases, Rev1, Pol [zeta], and Pol [eta], perform TLS in Saccharomyces cerevisiae. In addition to their contribution to cellular survival after DNA damage, Rev1 and Pol [zeta] are responsible for the majority of spontaneous and damage-induced mutagenesis. Thus mutagenesis, at least for Pol [zeta], is a consequence of a catalytic activity with an increased error rate relative to replicative polymerases like Pols [delta] and [epsilon].

Department dc:contributor.department

Massachusetts Institute of Technology. Dept. of Biology.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2009

Author dc:creator

• Wiltrout, Mary Ellen

Advisor dc:contributor.advisor

• Graham C. Walker.

• Biology.

Statement dc:rights

• M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/47884

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/47884